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HDL CHOLESTEROL REAGENT (PTA/MGCL2)

K890023 Class I Traditional
Decision Date
1989-02-17
Sponsor / Applicant
Sigma Diagnostics, Inc.

Technical Specification

510(k) Submission ID K890023
Product Code LBR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1989-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HDL CHOLESTEROL REAGENT (PTA/MGCL2) received FDA 510(k) clearance under submission number K890023, sponsored by Sigma Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1989-02-17.

Classification & Regulation

This clearance is catalogued under FDA product code LBR and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.